Literature DB >> 9060585

Adult polycystic liver disease: is fenestration the most adequate operation for long-term management?

J F Gigot1, P Jadoul, F Que, B E Van Beers, J Etienne, Y Horsmans, A Collard, A Geubel, J Pringot, P J Kestens.   

Abstract

OBJECTIVE: The aim of this study was to evaluate the immediate and long-term results in a retrospective series of patients with highly symptomatic adult polycystic liver disease (APLD) treated by extensive fenestration techniques. A classification of APLD was developed as a stratification scheme to help surgeons conceptualize which operation to offer to patients with APLD. SUMMARY BACKGROUND DATA: Treatment options for APLD remain controversial, with partisans of fenestration techniques or combined liver resection-fenestration.
METHODS: Clinical symptoms, performance status, liver volume measurement by computed tomography (CT), and morbidity were recorded before surgery and after surgery. Adult polycystic liver disease was classified according to the number, size, and location of liver cysts and the amount of remaining liver parenchyma. Follow-up was obtained by clinical and CT examinations in all patients.
RESULTS: Ten patients with highly symptomatic APLD were operated on using an extensive fenestration technique (by laparotomy in 8 patients and by laparoscopy in 2 patients, 1 of whom conversion to laparotomy was required). The mean preoperative liver volume was 7761 cm3. There was no mortality. Postoperative morbidity occurred in 50%, mainly from biliary complications, requiring reintervention in two cases. Massive intraoperative hemorrhage occurred in one patient. During a mean follow-up time of 71 months (range, 17 to 239 months), all patients were improved clinically according to their estimated performance status. The mean postoperative liver volume was 4596 cm3, which represents a mean liver volume reduction rate of 43%. However, in type III APLD, despite absence of clinical symptoms, a significant increase in liver volume was observed in 40% of the patients.
CONCLUSIONS: Extensive fenestration is effective in relieving symptoms in patients with APLD. Hemorrhage and biliary complications are possible consequences of such an aggressive attempt to reduce liver volume. The procedure can be performed laparoscopically in type I APLD. A longer follow-up period is mandatory in type II APLD, to confirm the usefulness of the fenestration procedure. In type III APLD, significant disease progression was observed in 40% of the patients during long-term follow-up. Fenestration may not be the most appropriate operation for long-term management of all types of APLD.

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Year:  1997        PMID: 9060585      PMCID: PMC1190679          DOI: 10.1097/00000658-199703000-00008

Source DB:  PubMed          Journal:  Ann Surg        ISSN: 0003-4932            Impact factor:   12.969


  55 in total

1.  Polycystic liver; analysis of seventy cases.

Authors:  P J MELNICK
Journal:  AMA Arch Pathol       Date:  1955-02

2.  Laparoscopic treatment of nonparasitic liver cysts: adequate selection of patients and surgical technique.

Authors:  J F Gigot; M Legrand; G Hubens; L de Canniere; E Wibin; F Deweer; M L Druart; C Bertrand; H Devriendt; R Droissart; M Tugilimana; P Hauters; L Vereecken
Journal:  World J Surg       Date:  1996-06       Impact factor: 3.352

3.  Jaundice associated with polycystic liver disease. Relief by surgical decompression of the cysts.

Authors:  R J Howard; R F Hanson; J P Delaney
Journal:  Arch Surg       Date:  1976-07

4.  Clinical experience with adult polycystic liver disease.

Authors:  J N Vauthey; G J Maddern; P Kolbinger; H U Baer; L H Blumgart
Journal:  Br J Surg       Date:  1992-06       Impact factor: 6.939

Review 5.  Surgery for adult polycystic liver disease.

Authors:  C Soravia; G Mentha; E Giostra; P Morel; A Rohner
Journal:  Surgery       Date:  1995-03       Impact factor: 3.982

6.  Bleeding oesophageal varices and hepatic dysfunction in adult polycystic kidney disease.

Authors:  P J Ratcliffe; S Reeders; J M Theaker
Journal:  Br Med J (Clin Res Ed)       Date:  1984-05-05

7.  Non-parasitic liver cysts and polycystic liver disease: results of surgical treatment.

Authors:  D Henne-Bruns; H J Klomp; B Kremer
Journal:  Hepatogastroenterology       Date:  1993-02

8.  Cholangiocellular carcinoma associated with multiple liver cysts.

Authors:  M Imamura; T Miyashita; T Tani; A Naito; T Tobe; K Takahashi
Journal:  Am J Gastroenterol       Date:  1984-10       Impact factor: 10.864

9.  Surgical management of nonparasitic cystic liver disease.

Authors:  H Sanchez; M Gagner; R L Rossi; R L Jenkins; W D Lewis; J L Munson; J W Braasch
Journal:  Am J Surg       Date:  1991-01       Impact factor: 2.565

10.  Choledochoscopic appearance of hepatic ducts in polycystic disease of the liver.

Authors:  B Heather; B S Ashby
Journal:  J R Soc Med       Date:  1978-07       Impact factor: 18.000

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8.  Laparoscopic fenestration of liver cysts in polycystic liver disease results in a median volume reduction of 12.5%.

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